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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 656 (1992), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 258 (1975), S. 751-754 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Neurones were penetrated with double-barrelled glass microelectrodes as previously described4'8'9. One barrel was used to record membrane potential and the other to pass d.c. or current pulses for measurement of membrane resistance. Drugs were iontophoresed using a five-barrelled extracellular ...
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 204 (1973), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
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  • 4
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 252 (1974), S. 483-485 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Abdominal, cerebral, pleural and pedal ganglia of Aplysia californica or Aplysia dactylomela were removed and pinned to Sylgard (Dow Corning) in a lucite 'chamber. The connective tissue capsule was slit with a razor blade to expose the cell bodies. Neurones were penetrated with a double barrelled ...
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 254 (1975), S. 343-344 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Histamine, originating primarily from mast cells, is an important pharmacological agent in the regulation of smooth muscle and visceral functions in mammals1. Two types of histamine receptor, Hx and H2, have been described. Activation of H! results principally in smooth muscle contraction and is ...
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular neurobiology 14 (1994), S. 591-597 
    ISSN: 1573-6830
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular neurobiology 20 (2000), S. 591-604 
    ISSN: 1573-6830
    Keywords: tin ; acetylcholine ; Lymnaea stagnalis L. ; membrane currents ; mollusks ; Na channel
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract 1. Inorganic tin and organotin compounds, occurring in aquatic ecosystems, are toxic and can cause behavioral abnormalities in living organisms. To determine the possible neuronal basis of these actions, the effects of both forms of Sn were studied on identified neurones of the mollusk, Lymnaea stagnalis L. 2. SnCl2 caused a dose-dependent decrease in the acetylcholine (Ach)-induced inward current. The effective threshold concentration, measured by a two microelectrode voltage clamp technique, was 0.1 μM, and the maximal effect occurred at 5 μM SnCl2. The depression of the inward current was greater after a 10 min preapplication (20%) than after 3 min treatment (7%). 3. The next series of experiments compared the actions of inorganic or organic tin compounds. In whole cell clamp experiments both (CH3)2SnCl2 and (CH3)3SnCl, like inorganic Sn, decreased the amplitude of Ach-induced current. Increasing the duration of the preapplication time resulted in an increase in the effect, but the action was not reversible. SnCl2 treatment caused a concentration-dependent alteration (initial potentiation followed by depression) of the amplitude of I Na(V) over the whole voltage range and slightly shifted the I–V curves to the left. In contrast, trimethyl tin decreased the amplitude of I Na(V) only at high concentration (100 μM). The activation time course of I Na was increased (τ = 0.43 ms in control and 0.55 ms in Sn), but Sn did not alter the inactivation parameters (τ = 3.43 and 3.41 ms). 4. These results support earlier findings that agonist- and voltage-activated channels are direct targets of toxic metals. We conclude that tin in both inorganic and organic forms acts at neuronal membranes to modulate synaptic transmission through direct actions on agonist-activated ion channels, and suggest that these actions may be the basis of the altered behavior of animals in tin-polluted environments.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular neurobiology 3 (1983), S. 329-344 
    ISSN: 1573-6830
    Keywords: D-600 ; acetylcholine receptors ; Aplysia ; ion channels ; voltage clamp
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary 1. The effects of the calcium channel blocker D-600 on the cation channels activated by acetylcholine (ACh) was studied in voltage-clampedAplysia neurons by voltage-jump relaxation analysis. 2. D-600 blocked the steady-state ACh current in a highly voltage-dependent manner, the degree of antagonism increasing with membrane hyperpolarization. 3. In the presence of D-600 the current relaxations following hyperpolarizing command steps became biphasic. The time constants of ACh-induced current relaxations (τ f), which approximate the mean channel lifetime, were reduced in a voltage-dependent manner, the degree of reduction ofτ f increasing with increasing membrane potential. 4. In addition to the acceleration ofτ f, a slow, inverse kinetic component (τ s) of the relaxation appeared in the presence of D-600. The rate of this inverse kinetic component was accelerated either by increasing the agonist or antagonist dose or by increasing the membrane potential. 5. These results suggest that D-600 acts to antagonize the acetylcholine response through a blockade of the open state of the transmitter-activated cation channel. Possible kinetic schemes for this interaction are discussed.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular neurobiology 4 (1984), S. 263-271 
    ISSN: 1573-6830
    Keywords: strychnine ; acetylcholine receptors ; Aplysia ; relaxation analysis ; isolated neurons
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary 1. The blocking actions of strychnine on excitatory acetylcholine (ACh) responses in isolated, voltage clampedAplysia neuronal cell bodies has been studied using a rapid drug application technique. 2. Rapid microperfusion of strychnine (10–50µM) produced a reduction of the steady-state ACh-induced inward current inAplysia neurons which decayed exponentially with a highly dose-dependent time constant. At the cessation of strychnine perfusion the ACh-induced current recovered to its original value with an exponential time course which was not sensitive to the dose of strychnine previously applied. 3. The calculated association (k 1) and dissociation (k -1) constants for a pseudo-first-order reaction between strychnine and its binding site werek 1 = 1.2 × 104 M −1 · sec−1 andk -1 = 0.12 sec−1 (K D = 1 × 10−5 M −1). 4. These results demonstrate that concentration jump relaxation experiments can be performed on isolated neurons for the study of voltage-independent antagonists by the use of rapid microperfusion systems and provide the first direct estimates to date of the rate constants of the cholinolytic effect of strychnine.
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  • 10
    ISSN: 1573-6830
    Keywords: pyriform cortex ; kainate ; quisqualate ; N-methyl aspartate ; ion channels ; zinc ; cobalt ; calcium ; magnesium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary 1. The actions of ionophoretically appliedN-methyl aspartate (NMA), quisqualate, and kainate, thought to activate three different types of excitatory amino acid receptors, were studied on pyramidal neurons of the rat pyriform cortex, maintained in an isolated, submerged, and perfused brain slice. Intracellular recordings were made with either K acetate or CsCl electrodes. 2. In most neurons all three agonists elicited monophasic responses which could be evoked at 20-sec intervals. Some neurons showed biphasic responses, most commonly to kainate but, on occasion, also for quisqualate. The slower component appeared to be correlated with excitotoxicity and, consequently, was difficult to study. As a result the kainate responses studied were from neurons selected for having a single component. 3. In neurons selected for having a linear current-voltage relationship or neurons loaded with Cs to suppress K conductance and linearize the current-voltage relationship, the average changes in resistance recorded during ionophoretic responses at resting potential were as follows: NMA, 131.2 ± 6.7% of control; kainate, 104.7 ± 5.8% of control; and quisqualate, 92.8 ± 2.8% of control. The magnitude and direction of the conductance change were very reproducible in any one neuron, but especially for kainate some cells showed clear conductance increases, while others showed clear conductance decreases. 4. Using CsCl electrodes it was possible to reduce K+ conductance and depolarize the neurons over a wider range. By passing depolarizing current it was possible to reverse the responses. The response to all three agonists reversed at the same depolarized potential. This observation indicates that while there are differences in the ionic channels associated with the three agonists at resting potential, the channels have similar properties at more depolarized potentials. 5. Responses to all three agonists were influenced by the concentrations of divalent cations in the perfusion medium. The NMA responses were most sensitive to Mg, increasing in amplitude in the absence of Mg and being depressed by Mg elevation. All responses were sensitive to Ca, with discharges being greatly increased by low Ca and depressed by high Ca. The kainate response was most sensitive to Ca concentration changes. 6. Unlike reports from other preparations the apparent conductance decreases to NMA were not altered by the perfusion of solutions with either no added Mg or no added Ca. 7. The NMA response was very much reduced in either Co (1–2mM) or Zn (100–200µM). In contrast, the quisqualate response was relatively insensitive to Co but was consistently increased in the presence of Zn. The kainate response was not consistently affected by either, although there was some variation in individual experiments. 8. These results are consistent with the hypothesis that there are at least three distinct types of receptors for the excitatory amino acids in pyriform cortex and that these receptors are associated with three distinct ionic channels. The channels have many similar properties but possibly differ in divalent cation binding sites which regulate conductance to other ions.
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